HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Leukemia induction after a single retroviral vector insertion in Evi1 or Prdm16.

Abstract
Insertional activation of cellular proto-oncogenes by replication-defective retroviral vectors can trigger clonal dominance and leukemogenesis in animal models and clinical trials. Here, we addressed the leukemogenic potential of vectors expressing interleukin-2 receptor common gamma-chain (IL2RG), the coding sequence required for correction of X-linked severe combined immunodeficiency. Similar to conventional gamma-retroviral vectors, self-inactivating (SIN) vectors with strong internal enhancers also triggered profound clonal imbalance, yet with a characteristic insertion preference for a window located downstream of the transcriptional start site. Controls including lentivirally transduced cells revealed that ectopic IL2RG expression was not sufficient to trigger leukemia. After serial bone marrow transplantation involving 106 C57Bl6/J mice monitored for up to 18 months, we observed leukemic progression of six distinct clones harboring gamma-retroviral long terminal repeat (LTR) or SIN vector insertions in Evi1 or Prdm16, two functionally related genes. Three leukemic clones had single vector integrations, and identical clones manifested with a remarkably similar latency and phenotype in independent recipients. We conclude that upregulation of Evi1 or Prdm16 was sufficient to initiate a leukemogenic cascade with consistent intrinsic dynamics. Our study also shows that insertional mutagenesis is required for leukemia induction by IL2RG vectors, a risk to be addressed by improved vector design.
AuthorsU Modlich, A Schambach, M H Brugman, D C Wicke, S Knoess, Z Li, T Maetzig, C Rudolph, B Schlegelberger, C Baum
JournalLeukemia (Leukemia) Vol. 22 Issue 8 Pg. 1519-28 (Aug 2008) ISSN: 1476-5551 [Electronic] England
PMID18496560 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA-Binding Proteins
  • MDS1 and EVI1 Complex Locus Protein
  • Mecom protein, mouse
  • Prdm16 protein, mouse
  • Transcription Factors
Topics
  • Animals
  • Bone Marrow Transplantation
  • DNA-Binding Proteins (genetics)
  • Genetic Vectors
  • Leukemia, Experimental (genetics)
  • MDS1 and EVI1 Complex Locus Protein
  • Mice
  • Mice, Inbred C57BL
  • Mutagenesis, Insertional
  • Polymerase Chain Reaction
  • Proto-Oncogenes (genetics)
  • Retroviridae (genetics)
  • Transcription Factors (genetics)
  • Transduction, Genetic
  • Up-Regulation

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: